ACR Meeting Abstracts

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Abstracts tagged "T Cell"

  • Abstract Number: 1513 • ACR Convergence 2021

    Control of T Cell Tolerance by the NR4A Family of Nuclear Receptors

    Ryosuke Hiwa1, Hailyn Nielsen1, James Mueller1 and Julie Zikherman2, 1University of California San Francisco, San Francisco, CA, 2UCSF Medical Center, San Francisco, CA

    Background/Purpose: Current therapies for autoimmune disease often lead to treatment-limiting immunosuppression. Selective manipulation of antigen (Ag)-specific immune responses could enhance our therapeutic approach. Targeting members…
  • Abstract Number: 0547 • ACR Convergence 2021

    Autologous Haematopoietic Stem Cell Transplantation for Systemic Sclerosis Results in Sustained Changes in Immunoregulatory T and NK Cells

    Ross Penglase, Malini Visweswaran, John Zaunders, Laila Girgis, David Ma and John Moore, St Vincent's Hospital, Sydney, Australia

    Background/Purpose: Autologous Haematopoietic Stem Cell Transplantation (AHSCT) is an effective treatment for severe systemic sclerosis (SSc). To date, mechanistic studies have indicated possible pro-regulatory and…
  • Abstract Number: 1514 • ACR Convergence 2021

    Age-related Metabolic Reprogramming of Memory CD4+ T Cells Is Associated with Reactive Oxygen Species-induced Immune Cell Dysfunction

    Yuling Chen1, Pierre-Louis Krau2, Pelle Löwe3, Moritz Pfeiffenberger4, Lisa Ehlers3, Alexandra Damerau4, Paula Hoff3, Frank Buttgereit5 and Timo Gaber4, 1Charité University Medicine Berlin, Berlin, Germany, 2Charit Universittsmedizin Berlin, corporate member of Freie Universitt Berlin, Humboldt-Universitt zu Berlin, and Berlin Institute of Health, Department of Rheumatology and Clinical Immunology, Berlin, Germany, 3Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt Universität zu Berlin, Department of Rheumatology and Clinical Immunology, Berlin, Germany, 4Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany, 5Charité – Universitätsmedizin Berlin, Berlin, Germany

    Background/Purpose: Inflamm-aging is a sterile, low-grade, chronic systemic inflammatory state characterized by an increase in proinflammatory cytokines involved in the development of most age-related diseases…
  • Abstract Number: 0692 • ACR Convergence 2021

    Immunophenotyping of Inclusion Body Myositis Blood T Cells: Pathogenic and Biomarker Implications

    Namita Goyal1, Jonathan Cauchi1, Tyler Irani1, Nadia Araujo1, Leo Wang2, Marie Wencel1, Vivian Li3, Steven Greenberg4 and Tahseen Mozaffar1, 1University of California Irvine, Irvine, CA, 2University of Washington, Seattle, WA, 3University of California, Irvine, CA, 4Brigham and Women's Hospital Department of Neurology, Boston, MA

    Background/Purpose: The recent discovery of highly differentiated, killer cell lectin-like receptor subfamily G member 1 (KLRG1)+ T cells in the muscle of inclusion body myositis…
  • Abstract Number: 1750 • ACR Convergence 2021

    Itolizumab, a Novel anti-CD6 Therapy, in Systemic Lupus Erythematosus Patients: Interim Safety Results from the Phase 1b EQUALISE Dose-escalation Study

    Kenneth Kalunian1, Richard Furie2, Jai Radhakrishnan3, Vandana Mathur4, Krishna Polu4, Stephen Connelly4, Joel Rothman4, Cherie Ng4, Leslie Chinn5, Maple Fung6, Dolca Thomas7 and Chaim Putterman8, 1UC San Diego, La Jolla, CA, 2Zucker School of Medicine at Hofstra/Northwell, Great Neck, NY, 3Columbia University, New York, NY, 4Equillium, Inc., La Jolla, CA, 5Equillium, Inc., South San Francisco, CA, 6Equillium, Inc., San Diego, CA, 7Equillium, Inc., Brooklyn, NY, 8Albert Einstein College of Medicine, Bronx, NY

    Background/Purpose: CD6, a co-stimulatory receptor predominantly expressed on T cells, promotes CD4+ T cell proliferation and differentiation into Th1/Th17 cells. The CD6 ligand, activated leukocyte…
  • Abstract Number: 0693 • ACR Convergence 2021

    Discovery of Antigen Specific CD4+ T Cells in Anti-HMGCR-positive Immune Mediated Necrotizing Myopathy

    Eleni Tiniakou1, Andrew Mammen2 and Erika Darrah1, 1Johns Hopkins University, Baltimore, MD, 2National Institutes of Health, Bethesda, MD

    Background/Purpose: Anti-3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR)-positive immune mediated necrotizing myopathy (anti-HMGCR+ IMNM) is a unique myopathy characterized by IgG autoantibodies against HMGCR and a strong…
  • Abstract Number: 0947 • ACR Convergence 2021

    Cytokine Competent Gut-joint Migratory T Cells Contribute to Inflammation in the Joint

    Adam Lefferts1, David Claypool1, Eric Norman1, Uma Kantheti1 and Kristine Kuhn2, 1University of Colorado, Anschutz Medical Campus, Aurora, CO, 2University of Colorado Anschutz Medical Campus, Aurora, CO

    Background/Purpose: Although studies have identified the presence of gut-associated cells in the enthesis of joints affected by spondyloarthritis, a direct link through cellular transit between…
  • Abstract Number: 0774 • ACR Convergence 2020

    Nr4a1-high Arthritogenic T Cells from SKG Mice Are Associated with Markers of Recent and Chronic Antigen-stimulation and an Altered T Cell Receptor Repertoire

    Judith Ashouri-Sinha1, Elizabeth McCarthy1, Steven Yu2, Chun Jimmie Ye1 and Arthur Weiss1, 1UNIVERSITY OF CALIFORNIA, SAN FRANCISCO, San Francisco, CA, 2UNIVERSITY OF CALIFORNIA, SAN FRANCISCO, San Francsico, CA

    Background/Purpose: T cells can either be activated through their T cell receptor (TCR) in an antigen-specific manner, or in response to cytokines. Identification of antigen-reactive…
  • Abstract Number: 1407 • ACR Convergence 2020

    Resolvin D5 Modulates Th17/Treg Cell Differentiation and Suppresses Osteoclastogenesis

    Hirotaka Yamada1, Jun Saegusa2, Sho Sendo3, Yo Ueda4, Takaichi Okano1, Yoshikazu Fujikawa5, Yuzuru Yamamoto6, Takumi Nagamoto1, Yoshihide Ichise1, Ikuko Naka1, Kengo Akashi7, Akira Onishi7, Masakazu Shinohara1 and Akio Morinobu7, 1Kobe University, Kobe, Japan, 2Department of Clinical Laboratory, Kobe University Hospital, Kobe, Japan, 3Kobe University, Kobe, 4Kobe UniversityRheumatology and Clinical Immunology, Kobe University Hospital, Kobe, Japan, 5Kobe University, Kobe city, Japan, 6Kobe University, Kobe-city, Japan, 7Rheumatology and Clinical Immunology, Kobe University Hospital, Kobe, Japan

    Background/Purpose: Over the last two decades, it has become increasingly clear that resolution of acute inflammation is not a passive process, but requires active modulation.…
  • Abstract Number: 1857 • ACR Convergence 2020

    KIR3DL2 Is Not Overexpressed on CD4+ T Cells and NK Cells in Patients with Axial Spondyloarthritis csDMARD and bDMARD Naive

    Guillaume Larid1, Sophie Trijau1, Clothilde Barral1, Pierre Lafforgue1 and Thao Pham2, 1Aix Marseille Univ, APHM, Rheumatology department, Marseille, France, 2Aix Marseille Univ, APHM, department of rheumatology, Marseille, France

    Background/Purpose: Overexpression of KIR3DL2 on CD4+ T-cells and NK-cells has been reported in patients with ankylosing spondylitis (AS) HLAB27+. We aimed to 1) analyse KIR3DL2…
  • Abstract Number: 0775 • ACR Convergence 2020

    T and B Cell Responses to Common Tenascin-C Peptides in RA

    JING Song1, Anja Schwenzer2, Sara Turcinov3, Alicia Wong2, Cliff Rims1, Lorena Rodriguez Martinez2, David Arribas-Layton4, Christina Gerstner5, Virginia Muir6, Jeffrey Carlin7, Kim Midwood2, Vivianne Malmström8, Eddie James1 and Jane Buckner1, 1Center for Translational Immunology, Benaroya Research Institute at Virginia Mason, Seattle, WA, 2Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom, 3Division of Rheumatology, Department of Medicine,Center for Molecular Medicine, Institutet, Stockholm, Sweden, 4Center for Translational Immunology, Benaroya Research Institute at Virginia Mason, Seattle, 5Division of Rheumatology, Department of Medicine,Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden, 6Center for Systems Immunology, Benaroya Research Institute at Virginia Mason, Seattle, WA, 7Department of Rheumatology, Virginia Mason Medical Center, Seattle, WA, 8Karolinska Institutet, Stockholm, Stockholms Lan, Sweden

    Background/Purpose: Although autoreactive CD4+ T cell and antibody responses against citrullinated antigens are known to contribute to loss of immune tolerance in rheumatoid arthritis (RA),…
  • Abstract Number: 1408 • ACR Convergence 2020

    Metabolic Reprogramming in Memory CD4+ T Cells Is Associated with Immune Cell Dysfunction During Aging

    Yuling Chen1, Yuanchun Ye2, Hao Wu3, Pierre-Louis Krauß1, Pelle Löwe1, Moritz Pfeiffenberger1, Lisa Ehlers1, Thomas Buttgereit4, Paula Hoff5, Frank Buttgereit6 and Timo Gaber1, 1Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Rheumatology and Clinical Immunology, Berlin, Germany, 2Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Hematology, Oncology and Tumor Immunology, Berlin, Germany, 3Julius-Maximilians Universität Würzburg, Institut für Systemimmunologie, Würzburg, Germany, 4Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Dermatology, Venerology, and Allergology, Berlin, Germany, 5Endokrinologikum Berlin, Rheumatologie, Berlin, Germany, 6Charité University Medicine, Berlin, Germany

    Background/Purpose: Inflamm-aging is a chronic, sterile, low-grade inflammatory status, characterized by an increase of proinflammatory cytokines which participate in the development of most age-related diseases…
  • Abstract Number: 1858 • ACR Convergence 2020

    Increased Proportion of TH17, TH22 and TC17 Cells and the Correlation to IL-22 and Clinical Parameters in Patients with Ankylosing Spondylitis from Northern Sweden

    Kristina Lejon1, Urban Hellman2, Lan Do2, Anjani Kumar2 and Helena Forsblad-d'Elia3, 1Department of Clinical microbiology, Infection and Immunology, Umeå University, Umeå, Sweden, 2Department of Public Health and Clinical Medicine, Rheumatology, Umeå, Sweden, 3Department of Public Health and Clinical Medicine/Rheumatology, Umeå University, Umeå, Vasterbottens Lan, Sweden

    Background/Purpose: Increased levels of TH17 and TH22 as well as TC17 and TC22 cells have previously been associated with ankylosing spondylitis (AS). The correlation between…
  • Abstract Number: 0837 • ACR Convergence 2020

    Deletion of miR-223 Exacerbates Lupus Nephritis by Targeting S1pr1 in Faslpr/lpr Mice

    Sumie Hiramatsu Asano1, Tomoyuki Mukai2, Yoshitaka Morita3 and Jun Wada4, 1Kawasaki Medical School/Department of Rheumatology, Kurashiki city, Japan, 2Kawasaki Medical School, Kurashiki-shi, Okayama, Japan, 3Kawasaki Medical School/Department of Rheumatology, Kurashiki, Okayama, Japan, 4Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences., Okayama city, Japan

    Background/Purpose: To identify new candidate genes regulated by micro RNAs (miRNAs) and involved in the pathogenesis of systemic lupus erythematosus (SLE), we integrated miRNA and…
  • Abstract Number: 1409 • ACR Convergence 2020

    Lack of Conventional Acinar Cells in the Salivary Gland Following Anti PD-L1 and anti-PD-1 Immune Checkpoint Inhibitor Therapy

    Sarah Pringle1, Bert van der Vegt1, Xiaoyan Wang1, Nico van Bakelen1, Arjan Vissink1, Frans Kroese2 and Hendrika Bootsma2, 1UMCG, Groningen, 2University Medical Centre Groningen, Groningen, Netherlands

    Background/Purpose: Salivary glands (SGs) can be damaged by immune checkpoint inhibitor (ICI) therapy. In patients with ICI-induced SG dysfunction, 60% progress to fulfill the ACR-EULAR…
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Embargo Policy

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM CT on October 25. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

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